» Articles » PMID: 28934488

De Novo Pathway-based Biomarker Identification

Overview
Specialty Biochemistry
Date 2017 Sep 22
PMID 28934488
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Gene expression profiles have been extensively discussed as an aid to guide the therapy by predicting disease outcome for the patients suffering from complex diseases, such as cancer. However, prediction models built upon single-gene (SG) features show poor stability and performance on independent datasets. Attempts to mitigate these drawbacks have led to the development of network-based approaches that integrate pathway information to produce meta-gene (MG) features. Also, MG approaches have only dealt with the two-class problem of good versus poor outcome prediction. Stratifying patients based on their molecular subtypes can provide a detailed view of the disease and lead to more personalized therapies. We propose and discuss a novel MG approach based on de novo pathways, which for the first time have been used as features in a multi-class setting to predict cancer subtypes. Comprehensive evaluation in a large cohort of breast cancer samples from The Cancer Genome Atlas (TCGA) revealed that MGs are considerably more stable than SG models, while also providing valuable insight into the cancer hallmarks that drive them. In addition, when tested on an independent benchmark non-TCGA dataset, MG features consistently outperformed SG models. We provide an easy-to-use web service at http://pathclass.compbio.sdu.dk where users can upload their own gene expression datasets from breast cancer studies and obtain the subtype predictions from all the classifiers.

Citing Articles

A unified mediation analysis framework for integrative cancer proteogenomics with clinical outcomes.

Huang L, Long J, Irajizad E, Doecke J, Do K, Ha M Bioinformatics. 2023; 39(1).

PMID: 36648331 PMC: 9879726. DOI: 10.1093/bioinformatics/btad023.


A Robust Personalized Classification Method for Breast Cancer Metastasis Prediction.

Adnan N, Najnin T, Ruan J Cancers (Basel). 2022; 14(21).

PMID: 36358745 PMC: 9658757. DOI: 10.3390/cancers14215327.


Molecular Subclassification Based on Crosstalk Analysis Improves Prediction of Prognosis in Colorectal Cancer.

Liu X, Su L, Li J, Ou G Front Genet. 2021; 12:689676.

PMID: 34804112 PMC: 8600263. DOI: 10.3389/fgene.2021.689676.


A Network-Based Methodology to Identify Subnetwork Markers for Diagnosis and Prognosis of Colorectal Cancer.

Al-Harazi O, Kaya I, El Allali A, Colak D Front Genet. 2021; 12:721949.

PMID: 34790220 PMC: 8591094. DOI: 10.3389/fgene.2021.721949.


Transcriptional landscape of cellular networks reveal interactions driving the dormancy mechanisms in cancer.

Uzuner D, Akkoc Y, Peker N, Pir P, Gozuacik D, Cakir T Sci Rep. 2021; 11(1):15806.

PMID: 34349126 PMC: 8339123. DOI: 10.1038/s41598-021-94005-x.


References
1.
Alcaraz N, Friedrich T, Kotzing T, Krohmer A, Muller J, Pauling J . Efficient key pathway mining: combining networks and OMICS data. Integr Biol (Camb). 2012; 4(7):756-64. DOI: 10.1039/c2ib00133k. View

2.
Yersal O, Barutca S . Biological subtypes of breast cancer: Prognostic and therapeutic implications. World J Clin Oncol. 2014; 5(3):412-24. PMC: 4127612. DOI: 10.5306/wjco.v5.i3.412. View

3.
You Y, Rustin R, Sullivan J . Oncotype DX(®) colon cancer assay for prediction of recurrence risk in patients with stage II and III colon cancer: A review of the evidence. Surg Oncol. 2015; 24(2):61-6. DOI: 10.1016/j.suronc.2015.02.001. View

4.
Subramanian A, Tamayo P, Mootha V, Mukherjee S, Ebert B, Gillette M . Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc Natl Acad Sci U S A. 2005; 102(43):15545-50. PMC: 1239896. DOI: 10.1073/pnas.0506580102. View

5.
Diaz-Uriarte R . GeneSrF and varSelRF: a web-based tool and R package for gene selection and classification using random forest. BMC Bioinformatics. 2007; 8:328. PMC: 2034606. DOI: 10.1186/1471-2105-8-328. View